Solvent extraction of Cu,Mo, V,and U from leach solutions of copper ore and flotation tailings

A micro-cloud point extraction method was discussed for preconcentration and spectrophotometric quantification of U(VI). The method depends on complex formation between U(VI) and 2-(4-sulphophenyloazo)-1,8-dihydroxy-3,6-naphtalenedisulphonic acid (SPADNS) at pH 7.0 and subsequent extraction of the complex in a mixed surfactant medium (cethyltrimethyl ammonium bromide and Triton X-114). The separation was carried out in the presence of 1% Na₂SO₄ at room temperature. The calibration curve was linear up to 3000 µg L^?1. The enrichment factor, detection limit and precision were 16.0, 1.05 µg L^?1, and 2.3%, respectively. The method was employed for the determination of U(VI) in real samples with different matrices.     

Leak testing of carbon–tin nanocomposites by thermal analysis methods

Electrode materials consisted of tin nanograins encapsulated in different origin carbon buffer matrix (starch or water soluble polymer) were obtained in a simple and inexpensive process. The tin precursor was synthesized using modified reverse nanoemulsion technique (w/o) and then coated by a source of carbon. The composites precursors were pyrolysed, affording formation of C/Sn anode materials. The resulting samples were investigated by powder X-ray diffraction studies in order to verify the structure and calculate crystallites sizes. The morphology of the nanocomposites was characterized by low-temperature nitrogen adsorption method (N₂-BET). Thermal analysis measurements (EGA-TG/DTG/DTA and DSC) allowed determining optimal conditions of preparation process and estimating carbon content in the obtained anode materials. Thermogravimetric studies also proved to be highly useful in establishing the leak behaviour of C/Sn nanocomposites. The electrochemical performance of the nanopowders was examined by charge–discharge tests in R2032-type coin cell. The thermal analysis results as well as low-temperature nitrogen adsorption data indicated that the origin of carbon precursor has major impact on morphology and leak behaviour of the obtained carbon buffer matrix. The electrochemical tests showed that better tightness of carbon–tin nanocomposites resulted in higher gravimetric capacity and better cell performance.     

Structure and thermal properties of the fritted glazes in SiO<Subscript>2</Subscript>–Al<Subscript>2</Subscript>O<Subscript>3</Subscript>–CaO–MgO–Na<Subscript>2</Subscript>O–K<Subscript>2</Subscript>O–ZnO system

In this work, the structure and thermal properties of aluminosilicate fritted glazes in SiO₂–Al₂O₃–CaO–MgO–Na₂O–K₂O–ZnO system with (4.0 mol%) and without addition of ZnO were examined by GIXRD, FTIR, MAS-NMR and thermal methods (DTA, DIL). It has been found that the all experimental glazes are amorphous material (transparent glazes). On the base of spectroscopic investigations, it was found that zinc ions exist in the network glazes in the octahedral coordination—Zn²⁺ ions play a network modifier role in structure of glazes. An analysis of the data obtained from thermal tests showed that addition of ZnO into chemical composition results in decrease in glass transition temperature value (T _g) for all glazes (DTA, DIL). The coefficient of thermal expansion (α) is decreased as the whole measurement range for one series of fritted glazes.     

Analytical Strategy for the Determination of Selenium in Biological Materials by Inductively Coupled Plasma-Mass Spectrometry with a Dynamic Reaction Cell

Selenium was determined in serum, hair, and tobacco by inductively coupled plasma-mass spectrometry using ⁷⁷Se, ⁷⁸Se, and ⁸²Se. The set of standards method (SSM) and the standard addition method (SAM) were applied to calibration with and without the use of internal standards (⁷²Ge and ¹⁰³Rh). In addition, the usefulness of the dynamic reaction cell (DRC) with methane as the reaction gas was characterized. The results obtained in different conditions were evaluated in terms of precision and accuracy. It was demonstrated theoretically and experimentally that an internal standard is a potential source of systematic errors as it can be influenced multiplicatively and additively by its own interferents (independently of selenium). Furthermore, it was shown that—against common opinion—an internal standard can fail in elimination of chemical interference effects influencing selenium and in increasing of precision of selenium determinations. The DRC was shown to be effective in the elimination of additive effects, although the results obtained by both SSM and SAM with DRC were systematically positively erroneous. Finally, selenium was determined accurately in each examined sample when SAM was applied to calibration, and signals were measured either for ⁸²Se without the use of the DRC, or for ⁷⁷Se or ⁷⁸Se with the use of the DRC. In addition, it has also been shown that samples should be diluted prior to analysis to the greatest acceptable extent.     

A luminescence probe for measurements of electron-exchange rates in polymer films on electrodes

The effect of metal ions on the, reduction of 1,10-phenanthroline-5,6-quinone (1), 5,8-quinolinequinone (II) and 6,7-dichloro-5, 8-quinolinequinone (III) has been investigated in 50% dimethylsulfoxide+water solvent. 1 contains the 1,10-phenanthroline structure in both its quinone and hydroquinone forms, while II and III contain the 8-hydroxyquinoline structure in the hydroquinone forms. Complexation of the hydroquinones of II and III by metal ions causes positive shifts in the quinone half-wave potentials. These shifts have been used to calculate conditional formation constants for Pb²⁺(II) and Pb²⁺ and Zn²⁺(III). The quinone form of I binds strongly to Ni²⁺, Co²⁺ and Zn²⁺ but not to Ca²⁺. Mg²⁺. Mg₂₊. Mn²⁺ and Pb²⁺. With the latter four metals, binding to the hydroquinone from of I was detected and formation constants were determined. In addition to binding both the quinone and hydroquinone forms at the nitrogen atoms, Ni₂₊ Co²⁺ and Zn²⁺ formed complexes at the 1,2-dihydroxy site of the hydroquinone of I.     

Pointwise versus equal (quasi-normal) convergence via ideals

We prove a characterization showing when the ideal pointwise convergence does not imply the ideal equal (aka quasi-normal) convergence. The characterization is expressed in terms of a cardinal coefficient related to the bounding number b$\mathfrak{b}$. We also prove a characterization showing when the ideal equal limit is unique.     

On Nash approximation of complex analytic sets in Runge domains

We prove that every complex analytic set X in a Runge domain Ω   can be approximated by Nash sets on any relatively compact subdomain _Ω0${\Omega }_0$ of Ω. Moreover, for every Nash subset Y of Ω   with Y⊂X$Y\subset X$, the approximating sets can be chosen so that they contain Y∩_Ω0$Y\cap {\Omega }_0$. As a consequence, we derive a necessary and sufficient condition for a complex analytic set X to admit a Nash approximation which coincides with X along its arbitrary given subset.     

On spatial contagion and multivariate GARCH models

We propose a method for defining and measuring spatial contagion between two financial markets via conditional copulas. Some theoretical results on monotonicity and asymptotic properties of Gaussian copulas with respect to conditioning are presented. Next, we combine the spatial contagion approach with time series models. We investigate which model from a large family of multivariate GARCH is the best tool for modelling spatial contagion. In an empirical study, we show that among models designed for general fit, a two‐step model fitting procedure reduces the ability to describe the contagion effect. This is a feature of copula‐GARCH models. Copyright © 2013 John Wiley & Sons, Ltd.